| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Julie Ahringer | Q15709495 |
| Susan M. Gasser | Q21062334 | ||
| P2860 | cites work | A role for the malignant brain tumour (MBT) domain protein LIN-61 in DNA double-strand break repair by homologous recombination | Q21144893 |
| Transdifferentiation. Sequential histone-modifying activities determine the robustness of transdifferentiation | Q24302015 | ||
| A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation | Q24304870 | ||
| Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases | Q24315937 | ||
| HP1a: a structural chromosomal protein regulating transcription | Q27021442 | ||
| Histone methylation restrains the expression of subtype-specific genes during terminal neuronal differentiation in Caenorhabditis elegans | Q27318351 | ||
| Transcriptional repression of Hox genes by C. elegans HP1/HPL and H1/HIS-24 | Q27331769 | ||
| H4K20me1 contributes to downregulation of X-linked genes for C. elegans dosage compensation | Q27331824 | ||
| The C. elegans H3K27 demethylase UTX-1 is essential for normal development, independent of its enzymatic activity | Q27334177 | ||
| Systems Level Analysis of Histone H3 Post-translational Modifications (PTMs) Reveals Features of PTM Crosstalk in Chromatin Regulation | Q39682740 | ||
| An Argonaute transports siRNAs from the cytoplasm to the nucleus. | Q39752627 | ||
| HP1 binding to native chromatin in vitro is determined by the hinge region and not by the chromodomain | Q39777525 | ||
| The spatial dynamics of tissue-specific promoters during C. elegans development | Q40014678 | ||
| Perinuclear Anchoring of H3K9-Methylated Chromatin Stabilizes Induced Cell Fate in C. elegans Embryos. | Q40274527 | ||
| Heterochromatin protein 1 (HP1) modulates replication timing of the Drosophila genome | Q40784286 | ||
| Small regulatory RNAs inhibit RNA polymerase II during the elongation phase of transcription. | Q41473315 | ||
| Defining heterochromatin in C. elegans through genome-wide analysis of the heterochromatin protein 1 homolog HPL-2. | Q41735227 | ||
| Antagonism between MES-4 and Polycomb repressive complex 2 promotes appropriate gene expression in C. elegans germ cells | Q41960310 | ||
| Removal of Polycomb repressive complex 2 makes C. elegans germ cells susceptible to direct conversion into specific somatic cell types. | Q42426927 | ||
| Systematic identification of methyllysine-driven interactions for histone and nonhistone targets | Q42909185 | ||
| HP1 binding to chromatin methylated at H3K9 is enhanced by auxiliary factors | Q42951883 | ||
| Gene repression. H3K27me and PRC2 transmit a memory of repression across generations and during development | Q43015490 | ||
| The polycomb complex protein mes-2/E(z) promotes the transition from developmental plasticity to differentiation in C. elegans embryos. | Q43115568 | ||
| HP1(Swi6) mediates the recognition and destruction of heterochromatic RNA transcripts | Q43908593 | ||
| MORC-1 Integrates Nuclear RNAi and Transgenerational Chromatin Architecture to Promote Germline Immortality | Q46543801 | ||
| Antagonistic functions of SET-2/SET1 and HPL/HP1 proteins in C. elegans development | Q46925893 | ||
| The MES-2/MES-3/MES-6 complex and regulation of histone H3 methylation in C. elegans | Q47068688 | ||
| Step-wise methylation of histone H3K9 positions heterochromatin at the nuclear periphery. | Q47068818 | ||
| The C. elegans HP1 homologue HPL-2 and the LIN-13 zinc finger protein form a complex implicated in vulval development | Q47068972 | ||
| Two C. elegans histone methyltransferases repress lin-3 EGF transcription to inhibit vulval development | Q47069021 | ||
| The C. elegans Mi-2 chromatin-remodelling proteins function in vulval cell fate determination. | Q47069081 | ||
| Unique and redundant functions of C. elegans HP1 proteins in post-embryonic development | Q47069207 | ||
| MEP-1 and a homolog of the NURD complex component Mi-2 act together to maintain germline-soma distinctions in C. elegans | Q47069337 | ||
| Coordinated regulation of active and repressive histone methylations by a dual-specificity histone demethylase ceKDM7A from Caenorhabditis elegans | Q47069385 | ||
| Perinuclear distribution of heterochromatin in developing C. elegans embryos | Q47069593 | ||
| Whole-genome sequencing and variant discovery in C. elegans. | Q47595683 | ||
| Transgenerational transmission of environmental information in C. elegans | Q48251389 | ||
| Histone H3K9 methylation is dispensable for Caenorhabditis elegans development but suppresses RNA:DNA hybrid-associated repeat instability. | Q50278958 | ||
| Lamin-Binding Proteins in Caenorhabditis elegans. | Q50540028 | ||
| The RNAi Inheritance Machinery of Caenorhabditis elegans. | Q50987178 | ||
| Somatic misexpression of germline P granules and enhanced RNA interference in retinoblastoma pathway mutants. | Q52043143 | ||
| Polycomb group regulation of Hox gene expression in C. elegans. | Q52104494 | ||
| Multiple intercellular signalling systems control the development of the Caenorhabditis elegans vulva. | Q52236554 | ||
| Conserved antagonism between JMJD2A/KDM4A and HP1γ during cell cycle progression. | Q53284482 | ||
| Repetitive Transgenes in C. elegans Accumulate Heterochromatic Marks and Are Sequestered at the Nuclear Envelope in a Copy-Number- and Lamin-Dependent Manner | Q61275222 | ||
| The kinetochores of Caenorhabditis elegans | Q70598101 | ||
| SynMuv genes redundantly inhibit lin-3/EGF expression to prevent inappropriate vulval induction in C. elegans | Q83296442 | ||
| The Nrde Pathway Mediates Small-RNA-Directed Histone H3 Lysine 27 Trimethylation in Caenorhabditis elegans | Q86127390 | ||
| Satellite DNAs between selfishness and functionality: structure, genomics and evolution of tandem repeats in centromeric (hetero)chromatin. | Q37053228 | ||
| HPL-2/HP1 prevents inappropriate vulval induction in Caenorhabditis elegans by acting in both HYP7 and vulval precursor cells | Q37102700 | ||
| Mapping H4K20me3 onto the chromatin landscape of senescent cells indicates a function in control of cell senescence and tumor suppression through preservation of genetic and epigenetic stability. | Q37125884 | ||
| A C. elegans LSD1 demethylase contributes to germline immortality by reprogramming epigenetic memory | Q37166371 | ||
| Heterochromatin protein 1 is recruited to various types of DNA damage. | Q37263966 | ||
| Amplification of siRNA in Caenorhabditis elegans generates a transgenerational sequence-targeted histone H3 lysine 9 methylation footprint | Q37359550 | ||
| The shelterin protein POT-1 anchors Caenorhabditis elegans telomeres through SUN-1 at the nuclear periphery | Q37379029 | ||
| Stable Caenorhabditis elegans chromatin domains separate broadly expressed and developmentally regulated genes | Q37417986 | ||
| Regulation of the X chromosomes in Caenorhabditis elegans | Q37618160 | ||
| Function, targets, and evolution of Caenorhabditis elegans piRNAs | Q37633703 | ||
| Decoupling the downstream effects of germline nuclear RNAi reveals that H3K9me3 is dispensable for heritable RNAi and the maintenance of endogenous siRNA-mediated transcriptional silencing in Caenorhabditis elegans | Q37644161 | ||
| Caenorhabditis elegans as a model system for studying the nuclear lamina and laminopathic diseases | Q37942334 | ||
| Recognition of methylated histones: new twists and variations | Q37953134 | ||
| Molecular mechanisms and potential functions of histone demethylases | Q37999690 | ||
| What are memories made of? How Polycomb and Trithorax proteins mediate epigenetic memory | Q38206369 | ||
| Dynamic changes of histone H3 marks during Caenorhabditis elegans lifecycle revealed by middle-down proteomics | Q38401337 | ||
| New Insights into the Regulation of Heterochromatin | Q38785509 | ||
| Epigenetic balance of gene expression by Polycomb and COMPASS families | Q38852455 | ||
| JMJD-1.2/PHF8 controls axon guidance by regulating Hedgehog-like signaling | Q38996548 | ||
| H3K27 methylation: a promiscuous repressive chromatin mark | Q39035286 | ||
| Repression of germline RNAi pathways in somatic cells by retinoblastoma pathway chromatin complexes | Q27334718 | ||
| A pre-mRNA-associating factor links endogenous siRNAs to chromatin regulation | Q27336267 | ||
| Structure of the HP1 chromodomain bound to histone H3 methylated at lysine 9 | Q27638208 | ||
| Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 by Polycomb and HP1 chromodomains | Q27641772 | ||
| Role of the polycomb protein EED in the propagation of repressive histone marks | Q27657483 | ||
| Binding of different histone marks differentially regulates the activity and specificity of polycomb repressive complex 2 (PRC2) | Q27665361 | ||
| Histone methylation by PRC2 is inhibited by active chromatin marks | Q27667743 | ||
| Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 | ||
| Genome sequence of the nematode C. elegans: a platform for investigating biology | Q27860527 | ||
| Constitutive heterochromatin formation and transcription in mammals | Q28080683 | ||
| UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development | Q28241669 | ||
| The histone demethylase UTX enables RB-dependent cell fate control | Q28272073 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| Different Mi-2 complexes for various developmental functions in Caenorhabditis elegans | Q28475938 | ||
| H3K9me2/3 binding of the MBT domain protein LIN-61 is essential for Caenorhabditis elegans vulva development | Q28477443 | ||
| Increasing Notch signaling antagonizes PRC2-mediated silencing to promote reprograming of germ cells into neurons | Q28828201 | ||
| Occupying Chromatin: Polycomb Mechanisms for Getting to Genomic Targets, Stopping Transcriptional Traffic, and Staying Put | Q29301233 | ||
| How chromatin-binding modules interpret histone modifications: lessons from professional pocket pickers | Q29547350 | ||
| JmjC-domain-containing proteins and histone demethylation | Q29614517 | ||
| Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
| Large-scale sequencing reveals 21U-RNAs and additional microRNAs and endogenous siRNAs in C. elegans | Q29616062 | ||
| The Dfam database of repetitive DNA families | Q30488601 | ||
| Heterochromatic genome stability requires regulators of histone H3 K9 methylation | Q33422980 | ||
| Differential localization and independent acquisition of the H3K9me2 and H3K9me3 chromatin modifications in the Caenorhabditis elegans adult germ line | Q33526991 | ||
| A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress | Q33574854 | ||
| A histone methylation network regulates transgenerational epigenetic memory in C. elegans | Q33576338 | ||
| Partitioning the C. elegans genome by nucleosome modification, occupancy, and positioning | Q33587754 | ||
| The histone H3K36 methyltransferase MES-4 acts epigenetically to transmit the memory of germline gene expression to progeny. | Q33686906 | ||
| Reduced insulin/IGF-1 signaling restores germ cell immortality to Caenorhabditis elegans Piwi mutants | Q33724795 | ||
| Genome-wide analysis links emerin to neuromuscular junction activity in Caenorhabditis elegans. | Q33741805 | ||
| A heterochromatin protein 1 homologue in Caenorhabditis elegans acts in germline and vulval development | Q33757634 | ||
| DNA replication and transcription programs respond to the same chromatin cues. | Q33839410 | ||
| Distinct epigenomic landscapes of pluripotent and lineage-committed human cells. | Q33842527 | ||
| HP1alpha recruitment to DNA damage by p150CAF-1 promotes homologous recombination repair | Q33862272 | ||
| Chromatin regulation and sumoylation in the inhibition of Ras-induced vulval development in Caenorhabditis elegans | Q33899619 | ||
| Anchoring of Heterochromatin to the Nuclear Lamina Reinforces Dosage Compensation-Mediated Gene Repression. | Q36150010 | ||
| Extremely stable Piwi-induced gene silencing in Caenorhabditis elegans | Q36166738 | ||
| piRNAs can trigger a multigenerational epigenetic memory in the germline of C. elegans | Q36298021 | ||
| A nuclear Argonaute promotes multigenerational epigenetic inheritance and germline immortality | Q36433534 | ||
| A transgenerational role of the germline nuclear RNAi pathway in repressing heat stress-induced transcriptional activation in C. elegans | Q36466883 | ||
| An inverse relationship to germline transcription defines centromeric chromatin in C. elegans | Q36511978 | ||
| Mutation of C. elegans demethylase spr-5 extends transgenerational longevity | Q36559951 | ||
| H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans | Q36676559 | ||
| piRNAs initiate an epigenetic memory of nonself RNA in the C. elegans germline | Q36684944 | ||
| Enhancer of Rudimentary Cooperates with Conserved RNA-Processing Factors to Promote Meiotic mRNA Decay and Facultative Heterochromatin Assembly | Q36687330 | ||
| MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in the C. elegans germ line. | Q36731942 | ||
| PRG-1 and 21U-RNAs interact to form the piRNA complex required for fertility in C. elegans | Q36943578 | ||
| Two Conserved Histone Demethylases Regulate Mitochondrial Stress-Induced Longevity | Q36956854 | ||
| Gene regulation through nuclear organization. | Q36994161 | ||
| Position-effect variegation, heterochromatin formation, and gene silencing in Drosophila | Q37040262 | ||
| The epigenetics of germ-line immortality: lessons from an elegant model system | Q33903484 | ||
| Identification of grandchildless loci whose products are required for normal germ-line development in the nematode Caenorhabditis elegans | Q33958810 | ||
| Structural and functional dynamics of human centromeric chromatin | Q33996546 | ||
| Targeting X chromosomes for repression | Q34003258 | ||
| A C. elegans Piwi, PRG-1, regulates 21U-RNAs during spermatogenesis | Q34011879 | ||
| Piwi and piRNAs act upstream of an endogenous siRNA pathway to suppress Tc3 transposon mobility in the Caenorhabditis elegans germline | Q34012402 | ||
| DNA Methylation on N6-Adenine in C. elegans | Q34043905 | ||
| The protein encoded by the Drosophila position-effect variegation suppressor gene Su(var)3-9 combines domains of antagonistic regulators of homeotic gene complexes | Q34059541 | ||
| Nuclear compartmentalization and gene activity | Q34186324 | ||
| Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha | Q34196189 | ||
| R loops: from transcription byproducts to threats to genome stability | Q34271508 | ||
| Polycomb repressive complex 2 and H3K27me3 cooperate with H3K9 methylation to maintain heterochromatin protein 1α at chromatin | Q34297995 | ||
| Comparative analysis of metazoan chromatin organization | Q34486035 | ||
| Broad chromosomal domains of histone modification patterns in C. elegans | Q34548272 | ||
| Genomics in C. elegans: so many genes, such a little worm | Q34563189 | ||
| synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival | Q34592502 | ||
| Caenorhabditis elegans lin-13, a member of the LIN-35 Rb class of genes involved in vulval development, encodes a protein with zinc fingers and an LXCXE motif | Q34609776 | ||
| Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 | Q34613778 | ||
| Trans-generational epigenetic regulation of C. elegans primordial germ cells | Q34622455 | ||
| H3K36 methylation antagonizes PRC2-mediated H3K27 methylation | Q34624209 | ||
| The role of the Arabidopsis Exosome in siRNA-independent silencing of heterochromatic loci. | Q34650027 | ||
| Structures of SET domain proteins: protein lysine methyltransferases make their mark | Q34952892 | ||
| A PHF8 homolog in C. elegans promotes DNA repair via homologous recombination. | Q35326686 | ||
| HP1 and the dynamics of heterochromatin maintenance | Q35741016 | ||
| High evolutionary turnover of satellite families in Caenorhabditis. | Q35799797 | ||
| Two SET domain containing genes link epigenetic changes and aging in Caenorhabditis elegans | Q35836441 | ||
| LIN-61, one of two Caenorhabditis elegans malignant-brain-tumor-repeat-containing proteins, acts with the DRM and NuRD-like protein complexes in vulval development but not in certain other biological processes | Q35844907 | ||
| "Holo"er than thou: chromosome segregation and kinetochore function in C. elegans | Q35853959 | ||
| Caenorhabditis elegans Heterochromatin protein 1 (HPL-2) links developmental plasticity, longevity and lipid metabolism | Q35907679 | ||
| A Novel Epigenetic Silencing Pathway Involving the Highly Conserved 5'-3' Exoribonuclease Dhp1/Rat1/Xrn2 in Schizosaccharomyces pombe | Q35927018 | ||
| Heterochromatin protein 1, a known suppressor of position-effect variegation, is highly conserved in Drosophila | Q35935207 | ||
| The SynMuv genes of Caenorhabditis elegans in vulval development and beyond | Q35955994 | ||
| C. elegans piRNAs mediate the genome-wide surveillance of germline transcripts | Q36136040 | ||
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Caenorhabditis elegans | Q91703 |
| chromatin | Q180951 | ||
| P1104 | number of pages | 21 | |
| P304 | page(s) | 491-511 | |
| P577 | publication date | 2018-02-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Repressive Chromatin in Caenorhabditis elegans: Establishment, Composition, and Function | |
| P478 | volume | 208 |
| Q92227197 | Active chromatin marks drive spatial sequestration of heterochromatin in C. elegans nuclei |
| Q100395116 | Ancestral function of Inhibitors-of-kappaB regulates Caenorhabditis elegans development |
| Q90082889 | C. elegans synMuv B proteins regulate spatial and temporal chromatin compaction during development |
| Q83225257 | Diversification of the heat shock response by Helitron transposable elements |
| Q64923274 | H3.3K27M-induced chromatin changes drive ectopic replication through misregulation of the JNK pathway in C. elegans. |
| Q64901368 | Histone Methylation and Memory of Environmental Stress. |
| Q97874483 | Histone methyltransferase activity programs nuclear peripheral genome positioning |
| Q91595909 | LSM2-8 and XRN-2 contribute to the silencing of H3K27me3-marked genes through targeted RNA decay |
| Q89916726 | Lamina-Dependent Stretching and Unconventional Chromosome Compartments in Early C. elegans Embryos |
| Q92060510 | Mapping the dsRNA World |
| Q64055118 | Repression of Germline Genes in Somatic Tissues by H3K9 Dimethylation of Their Promoters |
| Q90193835 | The Epigenetics of Aging in Invertebrates |
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